Germ Cell Tumours Flashcards

1
Q

dont do this deck Are germ cell tumours common?

A

No, they are rare

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2
Q

What % of testicular tumours are germ cell tumours?

A

95%

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3
Q

What % of ovarian malignancies are germ cell tumours?

A

3-5%

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4
Q

When are germ cell tumours the most common cancer?

A

In men aged 20-40

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5
Q

When is the peak incidence of ovarian GCT?

A

Young women and adolescent girls

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6
Q

What % of GCT do extra-gonadal tumours account for?

A

Less than 10%

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7
Q

Where do extra-gonadal GCT occur?

A

In midline structures, most commonly in mediastinum and retroperitoneum, and rarely the brain, head, and neck

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8
Q

When is the peak incidence of GCT in the mediastinum?

A

3rd decade of life

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9
Q

What is the strongest risk factor for testicular GCTs?

A

Family history of testicular cancer

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10
Q

What are the other risk factors for testicular GCT?

A
  • History of maldescent
  • History of torsion
  • Kleinfelter’s syndrome
  • Atrophic testis
  • Previous testicular cancer
  • Infertility
  • In utero exposure to oestrogens
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11
Q

What genetic abnormality is found in more than 80% of testicular cancers?

A

12p gain, often as an isochromosome of 12p, where one arm of the chromosome is lost and replaced with an exact replica of the other arm

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12
Q

What is the precursor to testicular GCT?

A

Carcinoma in situ

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13
Q

What % of malignant GCT in men are seminomas?

A

50%

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14
Q

When is the peak incidence of seminomas?

A

30-40

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15
Q

When is spermatic seminoma more common?

A

Older men (60-70)

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16
Q

What female cancer is directly comparable with testicular seminomas?

A

Ovarian dysgerminoma

17
Q

What accounts for the majority of cases of ovarian GCTs?

A

Ovarian dysgerminoma

18
Q

What % of patients present with seminoma/dysgerminoma confined to the testis/ovary?

A

75%

19
Q

Describe the spread of seminoma/dysgerminoma?

A

It is usually predictable, from the para-aortic to supra-diaphragmatic nodes, and then to extranodal sites

20
Q

What is the result of the growth of seminoma/dysgerminoma being slow?

A

It may take up to 10 years to present clinically

21
Q

Do seminomas/dysgerminomas produce tumour markers?

A

They do not produce a reliable tumour marker, but hCG can be elevated in 10-25% of cases

22
Q

How do non-seminoma GCT compare to seminomas, in terms of spread?

A

Disease spread occurs earlier

23
Q

What is the result of disease spread occuring earlier in non-seminoma GCTs?

A

Only 50% of patients present with localised disease

24
Q

What tumour markers are associated with non-seminoma GCTs?

A

AFP and hCG

25
Q

What % of cases of non-seminoma GCTs have elevated AFP and hCP?

A

75%

26
Q

How do testicular GCTs present?

A
  • Painless solid mass in scrotum
  • Enlargement of testicle
  • Scrotal pain (i guess the actual lump doesnt hurt, but the scrotum does?)
  • Back pain
  • Dragging sensation in scrotum
  • Gynaecomastia
27
Q

What causes gynaecomastia in testicular GCTs?

A

High circulating hCG levels

28
Q

What might the presenting features of testicular GCTs be similar to?

A

Epididymo-orchitis

29
Q

When should epididymo-orchitis raise suspicion of testicular GCT?

A

If it does not respond to antibiotics